MYD88 Mutation Analysis

The myeloid differentiation primary response 88 gene (MYD88) encodes a cytosolic adapter protein, which acts as an essential signal transducer in the IL-1, IL-18 and Toll-like receptor signaling pathways and plays a central role in the innate and adaptive immune response. The MYD88 L265P mutation is a gain-of-function driver mutation that has been found in more than 90% of Waldenström macroglobulinemia (WM) / lymphoplasmacytic lymphoma (LPL) patients (1-3).  

The MYD88 L256P mutation detection kit was developed based on our eQ-PCR  platform, a proprietary technology that has high sensitivity and detects mutation(s) as low as 1% mutant allele frequency. 

  • A single tube test – simple procedure and clear results      
  • Detection of  MYD88 L265P mutation
  • Results in less than 1.5 hours
  • Works on any real-time PCR instrument

Assay information

Assay Format           One tube test.   
Assay Platform         Real time PCR machine
Assay Sensitivity      Detects 1-2% MYD88 L265P mutation
Sample required       20-100 ng DNA 

Order information
Cat. No. Product NameMutations Interrogated SizeDocuments
EP14eQ-PCR MYD88 Mutation AnalysisMYD88 L265P32 rxnManual

For research use only. Not for use in diagnostic procedures.

Example results:

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References

  1. Landgren O & Tageja N (2014). MYD88 and beyond: novel opportunities for diagnosis, prognosis and treatment in Waldenström's Macroglobulinemia. Leukemia. 28:1799. 
  2. Treon SP et al. (2012). MYD88 L265P somatic mutation in Waldenström’s macroglobulinemia. N Engl J Med. 367:826.
  3. Hamadeh F et al. (2015). MYD88 L265P mutation analysis helps define nodal lymphoplasmacytic lymphoma. Mod Pathol. 28:564.